Tablets were first developed in the mid-1850s, during which sugar coating (SC) was primarily used to improve their surface characteristics and protect pharmaceutical agents from the harsh environment ...

The pharmaceutical industry faces stringent regulatory requirements to ensure the safety, efficacy, and quality of drug products. Among these, Current Good Manufacturing Practice (CGMP) guidelines set ...

Pharmaceutical manufacturing requires defining quality target product profiles and critical quality attributes (CQAs) to ensure desired product quality. Process development identifies critical process ...

Technological innovations throughout the past several decades have transformed the pharmaceutical manufacturing process from traditional batch production to ...

A pharmaceutical tablet is defined as a solid dosage form containing drug material normally with suitable diluents and prepared either by compression or molding methods. Drug formulation and design ...

A CDMO championing a commitment to patients may sound like lip service or branding, but truly patient-centric CDMOs offer ...

Key information is needed for excipients and their potential impact on continuous manufacturing processes. An essential factor to consider when developing a robust continuous manufacturing (CM) ...

Raman Spectroscopy is an optical spectroscopy technique that provides a molecular fingerprint of a sample. Used as a practical analysis technique used inside and outside of the laboratory, Raman ...

In this course we examine powder properties and their role in these important processes, so that attendees can understand the influence of drug substance properties on formulation development how and ...

Global Pharmaceutical Manufacturing Equipment Market OverviewThe global pharmaceutical manufacturing equipment market is on a growth trajectory, projected to expand at a CAGR of 6–8% over the forecast ...